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(S)-(-)N-CARBOMETHOXY-ALPHA,ALPHA-DIPHENYL -2-PYRROLIDINEMETHANOL,98% is a chemical compound that is 98% pure and is an enantiomer of N-carbomethoxy-alpha,alpha-diphenyl-2-pyrrolidinemethanol. It has a specific three-dimensional arrangement of its atoms, which makes it a valuable chiral auxiliary in organic synthesis.
Used in Organic Synthesis:
(S)-(-)N-CARBOMETHOXY-ALPHA,ALPHA-DIPHENYL -2-PYRROLIDINEMETHANOL,98% is used as a chiral auxiliary for controlling the stereochemistry of a reaction. Its high level of purity makes it particularly useful in this application.
Used in Pharmaceutical Industry:
(S)-(-)N-CARBOMETHOXY-ALPHA,ALPHA-DIPHENYL -2-PYRROLIDINEMETHANOL,98% is used in the preparation of pharmaceutical compounds where stereochemistry is important. Its high purity ensures the quality and effectiveness of the resulting pharmaceuticals.

352535-68-3

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352535-68-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 352535-68-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,2,5,3 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 352535-68:
(8*3)+(7*5)+(6*2)+(5*5)+(4*3)+(3*5)+(2*6)+(1*8)=143
143 % 10 = 3
So 352535-68-3 is a valid CAS Registry Number.

352535-68-3 Well-known Company Product Price

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  • Aldrich

  • (554448)  Methyl(2S)-(−)-2-(hydroxydiphenylmethyl)-1-pyrrolidinecarboxylate  98%

  • 352535-68-3

  • 554448-500MG

  • 1,028.43CNY

  • Detail

352535-68-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl (2S)-2-[hydroxy(diphenyl)methyl]pyrrolidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:352535-68-3 SDS

352535-68-3Relevant academic research and scientific papers

Lanthanide Lewis acid-mediated enantioselective conjugate radical additions

Sibi, Mukund P.,Manyem, Shankar

, p. 2929 - 2932 (2007/10/03)

(figure presented) Lanthanide triflates along with proline-derived ligands have been found to be efficient catalysts for enantioselective conjugate addition of nucleophilic radicals to enoates. N-Acyl oxazolidinones, when used as achiral additives, gave meaningful enhancements in the ees for the product.

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